Sphingosine Kinase Interacts with TRAF2 and Dissects Tumor Necrosis Factor-α Signaling
Tumor necrosis factor-α (TNF) receptor-associated factor 2 (TRAF2) is one of the major mediators of TNF receptor superfamily transducing TNF signaling to various functional targets, including activation of NF-κB, JNK, and antiapoptosis. We investigated how TRAF2 mediates differentially the distinct...
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container_title | The Journal of biological chemistry |
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creator | Xia, Pu Wang, Lijun Moretti, Paul A.B. Albanese, Nathaniel Chai, Fugui Pitson, Stuart M. D'Andrea, Richard J. Gamble, Jennifer R. Vadas, Mathew A. |
description | Tumor necrosis factor-α (TNF) receptor-associated factor 2 (TRAF2) is one of the major mediators of TNF receptor superfamily transducing TNF signaling to various functional targets, including activation of NF-κB, JNK, and antiapoptosis. We investigated how TRAF2 mediates differentially the distinct downstream signals. We now report a novel mechanism of TRAF2-mediated signal transduction revealed by an association of TRAF2 with sphingosine kinase (SphK), a lipid kinase that is responsible for the production of sphingosine 1-phosphate. We identified a TRAF2-binding motif of SphK that mediated the interaction between TRAF2 and SphK resulting in the activation of the enzyme, which in turn is required for TRAF2-mediated activation of NF-κB but not JNK. In addition, by using a kinase inactive dominant-negative SphK and a mutant SphK that lacks TRAF2-binding motif we show that the interaction of TRAF2 with SphK and subsequent activation of SphK are critical for prevention of apoptosis during TNF stimulation. These findings show a role for SphK in the signal transduction by TRAF2 specifically leading to activation of NF-κB and antiapoptosis. |
doi_str_mv | 10.1074/jbc.M111423200 |
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We investigated how TRAF2 mediates differentially the distinct downstream signals. We now report a novel mechanism of TRAF2-mediated signal transduction revealed by an association of TRAF2 with sphingosine kinase (SphK), a lipid kinase that is responsible for the production of sphingosine 1-phosphate. We identified a TRAF2-binding motif of SphK that mediated the interaction between TRAF2 and SphK resulting in the activation of the enzyme, which in turn is required for TRAF2-mediated activation of NF-κB but not JNK. In addition, by using a kinase inactive dominant-negative SphK and a mutant SphK that lacks TRAF2-binding motif we show that the interaction of TRAF2 with SphK and subsequent activation of SphK are critical for prevention of apoptosis during TNF stimulation. These findings show a role for SphK in the signal transduction by TRAF2 specifically leading to activation of NF-κB and antiapoptosis.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M111423200</identifier><identifier>PMID: 11777919</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Apoptosis ; Blotting, Western ; Cell Line ; Cell Survival ; Cells, Cultured ; DNA, Complementary - metabolism ; Endothelium, Vascular - cytology ; Enzyme Activation ; Genes, Dominant ; Genes, Reporter ; Glutathione Transferase - metabolism ; Humans ; Models, Biological ; Mutagenesis, Site-Directed ; Mutation ; NF-kappa B - metabolism ; Phosphotransferases (Alcohol Group Acceptor) - chemistry ; Phosphotransferases (Alcohol Group Acceptor) - metabolism ; Plasmids - metabolism ; Precipitin Tests ; Protein Binding ; Proteins - chemistry ; Proteins - metabolism ; Recombinant Fusion Proteins - metabolism ; Signal Transduction ; Time Factors ; TNF Receptor-Associated Factor 2 ; Tumor Necrosis Factor-alpha - metabolism ; Umbilical Veins - cytology</subject><ispartof>The Journal of biological chemistry, 2002-03, Vol.277 (10), p.7996-8003</ispartof><rights>2002 © 2002 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-9edca853b1c79320032f9a0927b96e9c170f3e0e5eaa9d6f385b5f4943391eb23</citedby><cites>FETCH-LOGICAL-c425t-9edca853b1c79320032f9a0927b96e9c170f3e0e5eaa9d6f385b5f4943391eb23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11777919$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xia, Pu</creatorcontrib><creatorcontrib>Wang, Lijun</creatorcontrib><creatorcontrib>Moretti, Paul A.B.</creatorcontrib><creatorcontrib>Albanese, Nathaniel</creatorcontrib><creatorcontrib>Chai, Fugui</creatorcontrib><creatorcontrib>Pitson, Stuart M.</creatorcontrib><creatorcontrib>D'Andrea, Richard J.</creatorcontrib><creatorcontrib>Gamble, Jennifer R.</creatorcontrib><creatorcontrib>Vadas, Mathew A.</creatorcontrib><title>Sphingosine Kinase Interacts with TRAF2 and Dissects Tumor Necrosis Factor-α Signaling</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Tumor necrosis factor-α (TNF) receptor-associated factor 2 (TRAF2) is one of the major mediators of TNF receptor superfamily transducing TNF signaling to various functional targets, including activation of NF-κB, JNK, and antiapoptosis. 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These findings show a role for SphK in the signal transduction by TRAF2 specifically leading to activation of NF-κB and antiapoptosis.</description><subject>Apoptosis</subject><subject>Blotting, Western</subject><subject>Cell Line</subject><subject>Cell Survival</subject><subject>Cells, Cultured</subject><subject>DNA, Complementary - metabolism</subject><subject>Endothelium, Vascular - cytology</subject><subject>Enzyme Activation</subject><subject>Genes, Dominant</subject><subject>Genes, Reporter</subject><subject>Glutathione Transferase - metabolism</subject><subject>Humans</subject><subject>Models, Biological</subject><subject>Mutagenesis, Site-Directed</subject><subject>Mutation</subject><subject>NF-kappa B - metabolism</subject><subject>Phosphotransferases (Alcohol Group Acceptor) - chemistry</subject><subject>Phosphotransferases (Alcohol Group Acceptor) - metabolism</subject><subject>Plasmids - metabolism</subject><subject>Precipitin Tests</subject><subject>Protein Binding</subject><subject>Proteins - chemistry</subject><subject>Proteins - metabolism</subject><subject>Recombinant Fusion Proteins - metabolism</subject><subject>Signal Transduction</subject><subject>Time Factors</subject><subject>TNF Receptor-Associated Factor 2</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>Umbilical Veins - cytology</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEFOwzAQRS0EoqWwZYl8gRSPndTxsgIKFQUkWgS7yHEmras2qewUxLG4CGfCUSt1xWxGGv3_Nf8RcgmsD0zG18vc9J8AIOaCM3ZEusBSEYkEPo5JlzEOkeJJ2iFn3i9ZmFjBKekASCkVqC55n24WtprX3lZIH22lPdJx1aDTpvH0yzYLOnsdjjjVVUFvrffY3mfbde3oMxoXjJ6Ogrh20e8Pndp5pVch8JyclHrl8WK_e-RtdDe7eYgmL_fjm-EkMjFPmkhhYXSaiByMVG0DwUulmeIyVwNUBiQrBTJMUGtVDEqRJnlSxioWQgHmXPRIf5fbvuIdltnG2bV23xmwrCWUBULZgVAwXO0Mm22-xuIg3yMJgnQnwPD2p0WXeWOxMlhYF8pnRW3_y_4DAG50xA</recordid><startdate>20020308</startdate><enddate>20020308</enddate><creator>Xia, Pu</creator><creator>Wang, Lijun</creator><creator>Moretti, Paul A.B.</creator><creator>Albanese, Nathaniel</creator><creator>Chai, Fugui</creator><creator>Pitson, Stuart M.</creator><creator>D'Andrea, Richard J.</creator><creator>Gamble, Jennifer R.</creator><creator>Vadas, Mathew A.</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20020308</creationdate><title>Sphingosine Kinase Interacts with TRAF2 and Dissects Tumor Necrosis Factor-α Signaling</title><author>Xia, Pu ; Wang, Lijun ; Moretti, Paul A.B. ; Albanese, Nathaniel ; Chai, Fugui ; Pitson, Stuart M. ; D'Andrea, Richard J. ; Gamble, Jennifer R. ; Vadas, Mathew A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-9edca853b1c79320032f9a0927b96e9c170f3e0e5eaa9d6f385b5f4943391eb23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Apoptosis</topic><topic>Blotting, Western</topic><topic>Cell Line</topic><topic>Cell Survival</topic><topic>Cells, Cultured</topic><topic>DNA, Complementary - metabolism</topic><topic>Endothelium, Vascular - cytology</topic><topic>Enzyme Activation</topic><topic>Genes, Dominant</topic><topic>Genes, Reporter</topic><topic>Glutathione Transferase - metabolism</topic><topic>Humans</topic><topic>Models, Biological</topic><topic>Mutagenesis, Site-Directed</topic><topic>Mutation</topic><topic>NF-kappa B - metabolism</topic><topic>Phosphotransferases (Alcohol Group Acceptor) - chemistry</topic><topic>Phosphotransferases (Alcohol Group Acceptor) - metabolism</topic><topic>Plasmids - metabolism</topic><topic>Precipitin Tests</topic><topic>Protein Binding</topic><topic>Proteins - chemistry</topic><topic>Proteins - metabolism</topic><topic>Recombinant Fusion Proteins - metabolism</topic><topic>Signal Transduction</topic><topic>Time Factors</topic><topic>TNF Receptor-Associated Factor 2</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Umbilical Veins - cytology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xia, Pu</creatorcontrib><creatorcontrib>Wang, Lijun</creatorcontrib><creatorcontrib>Moretti, Paul A.B.</creatorcontrib><creatorcontrib>Albanese, Nathaniel</creatorcontrib><creatorcontrib>Chai, Fugui</creatorcontrib><creatorcontrib>Pitson, Stuart M.</creatorcontrib><creatorcontrib>D'Andrea, Richard J.</creatorcontrib><creatorcontrib>Gamble, Jennifer R.</creatorcontrib><creatorcontrib>Vadas, Mathew A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xia, Pu</au><au>Wang, Lijun</au><au>Moretti, Paul A.B.</au><au>Albanese, Nathaniel</au><au>Chai, Fugui</au><au>Pitson, Stuart M.</au><au>D'Andrea, Richard J.</au><au>Gamble, Jennifer R.</au><au>Vadas, Mathew A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sphingosine Kinase Interacts with TRAF2 and Dissects Tumor Necrosis Factor-α Signaling</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2002-03-08</date><risdate>2002</risdate><volume>277</volume><issue>10</issue><spage>7996</spage><epage>8003</epage><pages>7996-8003</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Tumor necrosis factor-α (TNF) receptor-associated factor 2 (TRAF2) is one of the major mediators of TNF receptor superfamily transducing TNF signaling to various functional targets, including activation of NF-κB, JNK, and antiapoptosis. We investigated how TRAF2 mediates differentially the distinct downstream signals. We now report a novel mechanism of TRAF2-mediated signal transduction revealed by an association of TRAF2 with sphingosine kinase (SphK), a lipid kinase that is responsible for the production of sphingosine 1-phosphate. We identified a TRAF2-binding motif of SphK that mediated the interaction between TRAF2 and SphK resulting in the activation of the enzyme, which in turn is required for TRAF2-mediated activation of NF-κB but not JNK. In addition, by using a kinase inactive dominant-negative SphK and a mutant SphK that lacks TRAF2-binding motif we show that the interaction of TRAF2 with SphK and subsequent activation of SphK are critical for prevention of apoptosis during TNF stimulation. These findings show a role for SphK in the signal transduction by TRAF2 specifically leading to activation of NF-κB and antiapoptosis.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11777919</pmid><doi>10.1074/jbc.M111423200</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Apoptosis Blotting, Western Cell Line Cell Survival Cells, Cultured DNA, Complementary - metabolism Endothelium, Vascular - cytology Enzyme Activation Genes, Dominant Genes, Reporter Glutathione Transferase - metabolism Humans Models, Biological Mutagenesis, Site-Directed Mutation NF-kappa B - metabolism Phosphotransferases (Alcohol Group Acceptor) - chemistry Phosphotransferases (Alcohol Group Acceptor) - metabolism Plasmids - metabolism Precipitin Tests Protein Binding Proteins - chemistry Proteins - metabolism Recombinant Fusion Proteins - metabolism Signal Transduction Time Factors TNF Receptor-Associated Factor 2 Tumor Necrosis Factor-alpha - metabolism Umbilical Veins - cytology |
title | Sphingosine Kinase Interacts with TRAF2 and Dissects Tumor Necrosis Factor-α Signaling |
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